Lilly Parenteral Responsible Engineer PFS in Sesto Fiorentino, Italy
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
The Senior Engineer in the Parenteral organization is a technical expert and an influential professional in the engineering function at Sesto.
He/she guarantees a secondary level technical support for Process Teams and Field Operations, being their technical reference and guide.
He/she is the point of contact for Sesto site inside the global network, representing the site in technical discussions and in project plans definition.
guarantees robust performance and reliability of production equipment, pursuing operational excellence
oversees that the equipment maintains the validated state, always assuring safety, quality and compliance to cGMPs
defines correct maintenance and recapitalization plans
drives continuous improvement of process and equipment, assuring compliance to latest internal and external rules and regulations
is the key contact point in the global network, technically representing the site
guarantees technical development of Process Engineers and Technicians by setting high standards, effective methodologies, data driven approach, pursuit of engineering fundamental principles
defines, prioritizes and implements a complex technical projects agenda
supports Process Teams and field operations being a technical mentor and leader
is a SME and the escalation point for technical discussions regarding equipment/processes/systems
is the contact person in case of regulatory or HSE inspections
proposes and evaluates new ideas or projects, defining accurate business cases and evaluating costs and resources need
leads complex investigations and coordinates troubleshooting and RCA
leads changes and process/equipment modifications
writes/reviews qualification documents, assessments, technical SOPs and instructions
owns technical documentation and drawings
encourages and leads technical sharing within and outside the site
owns the relations with technical third parties like equipment suppliers, directly managing service orders and contracts
Master degree in engineering (mechanical, electronic, industrial, automation, etc…)
5+ years experience in process engineering, maintenance, techincal support, process/equipment development
In depth technical proficiency on parenteral production plants and equipment
Good knowledge of cGMPs and pharma/HSE rules and standards
Exceptional capacity for managing simultaneous activities, competing priorities and challenges
Strong ability to work and communicate effectively with team and peers within a manufacturing and engineering organization. This includes excellent communication skills: written and verbal
Creative capacity for developing new ways to do things better, cheaper, faster
High level problem solving / root cause investigation skills
Leadership / influence
Prioritization & project management skills
Team player approach
Precision / thoroughness / broader view (see the “big picture”)
Creativity / thinking out of the box
Training / teaching / tutoring skills
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At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people. We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!